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Completed Phase 2 Interventional Results available

Rituximab to Treat Severe Hemophilia A

ClinicalTrials.gov ID: NCT00331006

Public ClinicalTrials.gov record NCT00331006. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 20, 2026, 12:51 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Rituximab for the Treatment of Inhibitors in Congenital Hemophilia A (A TMH CTN Study)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Hemophilia A is a serious blood clotting disorder caused by a lack of factor VIII, a specialized protein needed for normal blood clotting to occur. Individuals with this disease may experience spontaneous bleeding, pain and swelling in their joints due to excess bleeding, and bruising. A common treatment for severe hemophilia A is to intravenously replace the deficient blood clotting factor; however, some individuals may develop antibodies to this replacement factor. This study will evaluate the effectiveness of rituximab at reducing the antibodies that develop in response to the replacement factor in individuals with severe hemophilia A.

Study identification

NCT ID
NCT00331006
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Carelon Research
Other
Enrollment
23 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Months and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 31, 2006
Primary completion
Oct 31, 2010
Completion
Dec 31, 2011
Last update posted
Jun 10, 2013

2006 – 2012

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
Children's Hospital of Orange County Orange California 92868
Children's Healthcare of Atlanta Atlanta Georgia 30322
Rush University Medical Center Chicago Illinois 60612
Tulane University Health Sciences Center New Orleans Louisiana 70112
Children's Hospital Boston Boston Massachusetts 02115
UNC at Chapel Hill Hospital Chapel Hill North Carolina 27514
University Hospital of Cleveland Cleveland Ohio 44106
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104
Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104
Hemophilia Center of Western Pennsylvania Pittsburgh Pennsylvania 15213
University of Texas Southwestern Medical Center Dallas Texas 75390
Cook Children's Medical Center Fort Worth Texas 76104
Comprehensive Center for Bleeding Disorders Milwaukee Wisconsin 53201

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00331006, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 10, 2013 · Synced Sep 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00331006 live on ClinicalTrials.gov.

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